23 Security Manager Italy English-speaking jobs in Siena

to the Data Manager Coordinator. ... Philogen S.p.A. would like to hire a highly motivated and qualified Clinical Data Manager who will report

With 56,000 employees in 35 countries, including +2000 in Italy and 15,000 in Europe and Middle East, ... As a Store Manager, and a valued member of the Siena team, you will excel and enjoy this position if ... you are ready to actively handle the following missions: As a leader within Sephora Italy, the world's ... Collaborate with your Area Manager and the HR department in designing customized internal career development

With 56,000 employees in 35 countries, including +2000 in Italy and 15,000 in Europe and Middle East, ... Facilitate communication between the Store Manager and the Beauty Advisor team. ... Qualifications Minimum of 3-4 years of experience in similar roles (Assistant Store Manager, Team Leader

looking for a " GMP Sterility Assurance Specialist/Expert " who will report to the GMP Quality Assurance Manager

With 56,000 employees in 35 countries, including +2000 in Italy and 15,000 in Europe and Middle East, ... Facilitate communication between the Store Manager and the Beauty Advisor team. ... hesitate to apply if you have: Minimum of 3-4 years of experience in similar roles (Assistant Store Manager

Experienced Field Application Engineer/After-sales Engineer needed for BESS, PCS, and Lithium Battery Systems. Responsibilities include installation, commissioning, troubleshooting, maintenance, technical support, customer communication, training, and documentation. Requires a technical degree, 1-2 years of field service experience, and strong knowledge of relevant technologies.

Support the Store Manager and Specialists in managing daily activities.

Sales Manager for the Fitness Industry will generate leads, manage sales procedures, and onboard new members. Reports to the Director of Sales and Marketing. Requires 3 years of sales experience.

motivated and qualified "GMP Quality Assurance Specialist” who will report to the GMP Quality Assurance Manager

Overview The Computational and Translational Genomics Laboratory (CTGLab) at IIT-CNR, Pisa-Siena, Italy ... Duration : 1 year (renewable) Project : TRANSCAN-3 SeqPerGlio Location : CTGLab, IIT-CNR, Pisa-Siena, Italy

Job location Sovicille, Siena, Italy On-site position.

Lead clinical development for vaccine programs, including protocol design, report writing, and regulatory submissions. Oversee medical data listing and participate in safety review activities. Requires a Doctor of Medicine with an advanced degree and 2-3 years of industry experience or 10 years in a scientific institution.

The Tour Guy seeks a Marketing Content Coordinator to write, edit, and QA email campaigns and content for various channels. Requires 1+ year of experience in copywriting, email marketing, or content marketing. Must have hands-on experience with Klaviyo and strong organizational skills.

MAASI Enterprises seeks undergraduate or graduate students and recent graduates for a paid IT System Engineering internship. Interns will gain experience in software systems, regulatory requirements, technical documentation, and IT system support.

Process & Computer System Validation Specialist (GCP) will validate and maintain computerized systems ensuring compliance with GMP/GCP regulations. The role requires 2+ years of pharmaceutical experience, knowledge of computerized systems lifecycle, and regulatory frameworks (FDA 21 CFR Part 11, EU Annex 11, ISPE GAMP).

Finance Intern to support accounting, consolidation, and controlling activities at a biotechnology company.

MAASI Enterprises seeks final-year students or recent graduates for a paid internship in CSV, QA, Regulatory Affairs, and related fields. Interns will draft technical documentation, execute computerised systems testing, and support clients.

Archivist for Protected Categories Law 68/99 needed. Responsibilities include archiving, document management, and operational support for technical and scientific functions. Requires high school diploma, Microsoft Office proficiency, and experience in archiving, secretarial, or document management.

Qualification & Validation Specialist will prepare and verify qualification and validation documents, draft validation study protocols and reports, and execute qualification protocols and tests. Requires a degree in a relevant field, 3-4 years of pharmaceutical industry experience, and knowledge of GMP, risk-based methodologies, and validation procedures.

Philogen S.p.A. seeks a Medical Advisor to support the management and development of clinical trials in oncology and rheumatology. Responsibilities include contributing to trial design, execution, and analysis, providing expert guidance, and interacting with investigators and regulatory authorities.